Argon Medical Devices recalls its TRI-JECT 3-way IV organizer (REF 041230001A) due to potential incomplete pouch seals causing sterility loss. Affected units sold in 2023-2024.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
Argon Medical Devices is recalling its TRI-JECT 3-way IV administration organizer because the pouch seal might be incomplete, risking loss of sterility. This could lead to infections if used improperly.
The pouch seal may not form properly, allowing contaminants to enter the sterile product. This could cause infections during IV treatments if the device is not properly sterilized.
Healthcare professionals using the device for IV administration are most at risk. Patients receiving IV treatments with this device could face infection if sterility is compromised.
Check for the model number REF 041230001A on the label. The product was sold in boxes of 25, sterile, and distributed between 2023 and 2024.
Look for the model number REF 041230001A on the label to confirm if your device is affected.
The recall states the seal may be incomplete, which could lead to sterility loss. If you have the affected model, it should be checked for the seal issue before use.
Check for the model number REF 041230001A on the label. The product was sold in boxes of 25, sterile, and distributed between 2023 and 2024.
The recall does not specify a remedy, so contact Argon Medical Devices for guidance if you have the affected model.
We’ve drafted a message you can send Argon Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-0291-2020 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0291-2020 from Argon Medical Devices. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
